ENST00000489304.6:c.986G>T
|
ENSP00000512096.1:n.986G>T
|
|
ENST00000695675.1:n.2779G>T
|
|
|
ENST00000372285.8:c.*69G>T
MANE Select
|
ENSP00000361359.3:n.*69G>T
|
|
ENST00000372276.7:c.*229G>T
|
ENSP00000361350.3:n.*229G>T
|
|
ENST00000372285.7:c.*69G>T
|
ENSP00000361359.3:n.*69G>T
|
|
ENST00000466205.5:c.805G>T
|
|
|
ENST00000489304.5:n.979G>T
|
|
|
ENST00000620709.4:c.*450G>T
|
ENSP00000484074.1:n.*450G>T
|
|
NM_001250.5:c.*69G>T
|
NP_001241.1:n.*69G>T
|
|
NM_001302753.1:c.*229G>T
|
NP_001289682.1:n.*229G>T
|
|
NM_152854.3:c.*229G>T
|
NP_690593.1:n.*229G>T
|
|
NR_126502.1:n.996G>T
|
|
|
XM_005260617.2:c.*69G>T
|
XP_005260674.1:n.*69G>T
|
|
XM_005260619.2:c.*69G>T
|
XP_005260676.1:n.*69G>T
|
|
NM_001322421.1:c.*69G>T
|
NP_001309350.1:n.*69G>T
|
|
NM_001322422.1:c.*69G>T
|
NP_001309351.1:n.*69G>T
|
|
NM_001362758.1:c.*229G>T
|
NP_001349687.1:n.*229G>T
|
|
NR_136327.1:n.899G>T
|
|
|
XM_005260619.3:c.*69G>T
|
XP_005260676.1:n.*69G>T
|
|
XM_017028135.1:c.938G>T
|
XP_016883624.1:p.Cys313Phe
|
|
XM_017028136.1:c.836G>T
|
XP_016883625.1:p.Cys279Phe
|
|
NM_001250.6:c.*69G>T
MANE Select
|
NP_001241.1:n.*69G>T
|
|
NM_001302753.2:c.*229G>T
|
NP_001289682.1:n.*229G>T
|
|
NM_001322421.2:c.*69G>T
|
NP_001309350.1:n.*69G>T
|
|
NM_001322422.2:c.*69G>T
|
NP_001309351.1:n.*69G>T
|
|
NM_001362758.2:c.*229G>T
|
NP_001349687.1:n.*229G>T
|
|
NM_152854.4:c.*229G>T
|
NP_690593.1:n.*229G>T
|
|
NR_126502.2:n.936G>T
|
|
|
NR_136327.2:n.839G>T
|
|
|